Variant report

Variant	rs2872394
Chromosome Location	chr19:19171121-19171122
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	HEY1	chr19:19170629-19171496	K562	blood:	n/a	n/a
2	POLR2A	chr19:19170598-19171533	K562	blood:	n/a	n/a
3	STAT5A	chr19:19170656-19171516	K562	blood:	n/a	n/a
4	EGR1	chr19:19170911-19171346	K562	blood:	n/a	n/a
5	SP1	chr19:19170842-19171464	K562	blood:	n/a	chr19:19171412-19171426
6	ZNF274	chr19:19170865-19171346	K562	blood:	n/a	n/a
7	TEAD4	chr19:19169934-19171515	K562	blood:	n/a	n/a
8	EP300	chr19:19170714-19171350	K562	blood:	n/a	n/a
9	RAD21	chr19:19170921-19171271	K562	blood:	n/a	n/a
10	TAF7	chr19:19170974-19171315	K562	blood:	n/a	n/a
11	IRF1	chr19:19170305-19171363	K562	blood:	n/a	chr19:19171158-19171167
12	ETS1	chr19:19170814-19171413	K562	blood:	n/a	chr19:19171157-19171168
13	SP1	chr19:19170972-19171339	K562	blood:	n/a	n/a
14	CCNT2	chr19:19170719-19171430	K562	blood:	n/a	chr19:19171412-19171421 chr19:19171128-19171148
15	JUND	chr19:19170708-19171428	K562	blood:	n/a	n/a
16	CEBPB	chr19:19170790-19171393	K562	blood:	n/a	n/a
17	NR2F2	chr19:19169798-19172492	K562	blood:	n/a	chr19:19169852-19169867
18	POLR2A	chr19:19170521-19171344	PFSK-1	brain:	n/a	n/a
19	MYC	chr19:19170060-19172046	K562	blood:	n/a	n/a
20	CEBPD	chr19:19170664-19171501	K562	blood:	n/a	n/a
21	BHLHE40	chr19:19170754-19171379	K562	blood:	n/a	n/a
22	CEBPB	chr19:19170969-19171319	K562	blood:	n/a	n/a
23	RFX5	chr19:19170841-19171188	K562	blood:	n/a	n/a
24	RCOR1	chr19:19170630-19171412	K562	blood:	n/a	n/a
25	ATF1	chr19:19170973-19171366	K562	blood:	n/a	n/a
26	GATA1	chr19:19170829-19171358	K562	blood:	n/a	chr19:19171130-19171139 chr19:19171129-19171139 chr19:19171130-19171137 chr19:19171131-19171148
27	POLR2A	chr19:19170573-19171488	K562	blood:	n/a	n/a
28	HDAC2	chr19:19170860-19171401	K562	blood:	n/a	chr19:19171129-19171138
29	KAP1	chr19:19170923-19171391	K562	blood:	n/a	n/a
30	UBTF	chr19:19170866-19171373	K562	blood:	n/a	n/a
31	MYC	chr19:19170064-19172019	K562	blood:	n/a	n/a
32	SIX5	chr19:19171095-19171278	K562	blood:	n/a	n/a
33	MYC	chr19:19170608-19171337	K562	blood:	n/a	n/a
34	BCLAF1	chr19:19170618-19171410	K562	blood:	n/a	n/a
35	MAX	chr19:19170588-19171433	K562	blood:	n/a	n/a
36	GATA1	chr19:19170028-19171547	K562	blood:	n/a	chr19:19171130-19171139 chr19:19171129-19171139 chr19:19171130-19171137 chr19:19170170-19170180 chr19:19171131-19171148
37	ARID3A	chr19:19170863-19171339	K562	blood:	n/a	n/a
38	MAX	chr19:19169917-19171497	K562	blood:	n/a	n/a
39	TBL1XR1	chr19:19170702-19171422	K562	blood:	n/a	n/a
40	NR2F2	chr19:19170072-19171453	K562	blood:	n/a	n/a
41	YY1	chr19:19170787-19171515	K562	blood:	n/a	chr19:19171410-19171421
42	CUX1	chr19:19170674-19171249	K562	blood:	n/a	n/a
43	SPI1	chr19:19171028-19171235	K562	blood:	n/a	n/a
44	ZC3H11A	chr19:19171055-19171414	K562	blood:	n/a	n/a
45	GABPA	chr19:19170857-19171379	K562	blood:	n/a	n/a
46	IRF1	chr19:19170871-19171417	K562	blood:	n/a	chr19:19171158-19171167
47	CTCF	chr19:19170817-19171357	K562	blood:	n/a	n/a
48	ZNF143	chr19:19170822-19171336	K562	blood:	n/a	n/a
49	TBL1XR1	chr19:19170803-19171447	K562	blood:	n/a	n/a
50	POLR2A	chr19:19170018-19171460	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:19169646..19176603-chr19:19241603..19250623,23	K562	blood:
2	chr19:19171096..19173278-chr19:19281615..19284130,2	K562	blood:
3	chr19:19170341..19177029-chr19:19229928..19235464,11	K562	blood:
4	chr19:19170465..19178046-chr19:19213939..19220242,15	K562	blood:
5	chr19:19006431..19009212-chr19:19170311..19171914,2	K562	blood:
6	chr19:19170341..19172586-chr19:19233488..19235464,2	K562	blood:
7	chr19:19169419..19177029-chr19:19229685..19233171,13	K562	blood:
8	chr19:19141992..19145825-chr19:19171077..19177701,15	K562	blood:
9	chr19:19147736..19150233-chr19:19170434..19173422,2	K562	blood:
10	chr19:19170033..19172795-chr19:19186417..19188109,2	K562	blood:
11	chr19:19169646..19176667-chr19:19241603..19249514,19	K562	blood:

Variant related genes	Relation type
SLC25A42	TF binding region
ENSG00000130283	Chromatin interaction
ENSG00000223802	Chromatin interaction
ENSG00000105676	Chromatin interaction
ENSG00000064607	Chromatin interaction
ENSG00000064545	Chromatin interaction
ENSG00000181035	Chromatin interaction

Extended variants
information (count: 92 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs1007483	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs10221504	0.95[ASN][1000 genomes]
rs10403222	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10403322	0.83[EUR][1000 genomes]
rs10404627	0.95[ASN][1000 genomes]
rs10405189	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10405635	1.00[CHB][hapmap];0.90[JPT][hapmap];0.95[ASN][1000 genomes]
rs10409164	0.95[ASN][1000 genomes]
rs10410451	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10410568	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10414676	0.82[CEU][hapmap];0.85[CHB][hapmap];0.89[JPT][hapmap]
rs10416783	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10417974	0.85[CHB][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap]
rs10422335	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10422906	0.95[ASN][1000 genomes]
rs10423742	1.00[CHB][hapmap];1.00[CHD][hapmap];0.89[JPT][hapmap];0.95[ASN][1000 genomes]
rs10423815	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1079543	0.83[ASW][hapmap];0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.89[JPT][hapmap];0.86[LWK][hapmap];0.93[MEX][hapmap];0.97[TSI][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10854005	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1124921	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11666120	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11666340	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11666627	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11670204	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11670239	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11878368	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12016	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12975676	0.95[ASN][1000 genomes]
rs12975754	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12976302	0.92[ASN][1000 genomes]
rs12978822	0.89[ASN][1000 genomes]
rs12979565	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12985799	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1859267	0.83[ASW][hapmap];0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2012318	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.95[ASN][1000 genomes]
rs2107263	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2158320	1.00[ASN][1000 genomes]
rs2240094	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2240095	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2269806	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2269869	0.84[CEU][hapmap]
rs2285851	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2313736	0.97[ASN][1000 genomes]
rs3180770	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4808172	0.83[ASW][hapmap];0.90[CEU][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap];0.83[YRI][hapmap]
rs4808179	1.00[ASN][1000 genomes]
rs4808184	0.95[ASN][1000 genomes]
rs4808902	0.97[ASN][1000 genomes]
rs4808904	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4808905	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4808906	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4808907	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4808911	1.00[ASN][1000 genomes]
rs4808913	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4808916	1.00[CHB][hapmap];0.86[JPT][hapmap];0.95[ASN][1000 genomes]
rs6511010	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6511011	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6511014	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6511015	1.00[ASN][1000 genomes]
rs6511017	1.00[ASN][1000 genomes]
rs6511018	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.80[LWK][hapmap];0.95[ASN][1000 genomes]
rs6511021	0.82[CEU][hapmap];0.85[CHB][hapmap]
rs7248399	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs7248771	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7250131	0.95[ASN][1000 genomes]
rs7253244	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7255937	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7256648	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7257635	0.91[ASN][1000 genomes]
rs7258637	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7259510	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7259609	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs757220	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs8101529	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8103431	0.95[ASN][1000 genomes]
rs8104754	0.85[EUR][1000 genomes]
rs8104799	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8106146	0.86[CHB][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8107710	0.90[ASN][1000 genomes]
rs8109654	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8110629	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8111634	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8111635	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8112566	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs916898	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs929215	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9304959	1.00[ASN][1000 genomes]
rs9676917	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833778	chr19:19012669-19201487	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
2	nsv1059305	chr19:19131310-19209999	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
3	nsv543927	chr19:19147376-19178024	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
4	nsv833779	chr19:19163492-19313091	Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs2872394	TMEM161A	cis	Muscle Skeletal	GTEx
rs2872394	KIAA1683	cis	cerebellum	SCAN
rs2872394	NDUFA13	cis	parietal	SCAN
rs2872394	MED26	cis	cerebellum	SCAN
rs2872394	ZNF506	cis	parietal	SCAN

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:19145000-19174000	Weak transcription	Small Intestine	intestine
2	chr19:19145400-19171800	Weak transcription	Right Atrium	heart
3	chr19:19145600-19172200	Weak transcription	Stomach Mucosa	stomach
4	chr19:19145600-19173800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr19:19145600-19173800	Weak transcription	Fetal Kidney	kidney
6	chr19:19151000-19173800	Weak transcription	Fetal Brain Male	brain
7	chr19:19151800-19173800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr19:19151800-19173800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr19:19152600-19173200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr19:19152800-19171400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr19:19153200-19171200	Strong transcription	HUES64 Cell Line	embryonic stem cell
12	chr19:19153200-19171400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr19:19153200-19172200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr19:19153200-19173600	Strong transcription	Fetal Stomach	stomach
15	chr19:19153400-19171200	Strong transcription	Cortex derived primary cultured neurospheres	brain
16	chr19:19156600-19172800	Strong transcription	Dnd41	blood
17	chr19:19159800-19171400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr19:19160200-19172400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr19:19160400-19173000	Strong transcription	Thymus	Thymus
20	chr19:19160400-19173600	Strong transcription	Fetal Brain Female	brain
21	chr19:19161600-19171200	Strong transcription	Spleen	Spleen
22	chr19:19161600-19172400	Strong transcription	NHLF	lung
23	chr19:19161800-19172800	Strong transcription	Brain Germinal Matrix	brain
24	chr19:19162000-19171200	Strong transcription	Esophagus	oesophagus
25	chr19:19162000-19173000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr19:19162400-19172400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr19:19162800-19173800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr19:19163000-19172400	Strong transcription	Lung	lung
29	chr19:19164200-19171800	Weak transcription	Fetal Heart	heart
30	chr19:19164600-19171200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr19:19165200-19172400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr19:19165400-19172800	Weak transcription	Hela-S3	cervix
33	chr19:19165800-19173000	Weak transcription	NHDF-Ad	bronchial
34	chr19:19166000-19172800	Weak transcription	HUVEC	blood vessel
35	chr19:19166000-19173800	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr19:19166200-19173800	Weak transcription	Colon Smooth Muscle	Colon
37	chr19:19166400-19173800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr19:19166400-19174000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr19:19166600-19173400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr19:19166800-19172000	Weak transcription	HSMMtube	muscle
41	chr19:19167000-19172800	Weak transcription	NH-A	brain
42	chr19:19167000-19173800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr19:19167400-19173800	Genic enhancers	Fetal Muscle Trunk	muscle
44	chr19:19167400-19173800	Genic enhancers	Fetal Muscle Leg	muscle
45	chr19:19168400-19171200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr19:19168400-19172200	Weak transcription	HSMM	muscle
47	chr19:19168400-19173200	Weak transcription	A549	lung
48	chr19:19168600-19173200	Weak transcription	Primary hematopoietic stem cells	blood
49	chr19:19168600-19173200	Weak transcription	Osteobl	bone
50	chr19:19168600-19173800	Weak transcription	Primary B cells from cord blood	blood

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